15 positions on this site are linked to Unspecified Diffuse Connective Tissue Disease, out of 90,727 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
SPOP · rs182995751
See detailed info → SensitiveLRP11 · rs570063769
See detailed info → Sensitivenear LINC02183 · rs566347593
See detailed info → SensitivePCLO · rs187248060
See detailed info → Sensitivenear HDAC4 · rs183986544
See detailed info → Sensitivenear RPL34P27 · rs559354294
See detailed info → SensitivePFKP · rs138559816
See detailed info → SensitivePTGIS · rs548897351
See detailed info → SensitiveUIMC1 · rs542312023
See detailed info → Sensitivenear ELL2P3 · rs149527404
See detailed info → SensitiveTRIM55 · rs548960401
See detailed info → SensitiveKCNMB2 · rs189923567
See detailed info → Sensitivenear MIR3201 · rs139695700
See detailed info → Sensitivenear LPAR3 · rs562481287
See detailed info → Sensitivenear HHEX · rs182529846
See detailed info →One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.
The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.
No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.
Yes — the search box above matches gene symbols and rsIDs as well as trait names.